US6923189B2 - Cleaning of CVD chambers using remote source with cxfyoz based chemistry - Google Patents

Cleaning of CVD chambers using remote source with cxfyoz based chemistry Download PDF

Info

Publication number
US6923189B2
US6923189B2 US10/346,836 US34683603A US6923189B2 US 6923189 B2 US6923189 B2 US 6923189B2 US 34683603 A US34683603 A US 34683603A US 6923189 B2 US6923189 B2 US 6923189B2
Authority
US
United States
Prior art keywords
reactive species
processing chamber
chamber
carbon
fluorine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related, expires
Application number
US10/346,836
Other versions
US20040139983A1 (en
Inventor
Annamalai Lakshmanan
Ju-hyung Lee
Troy Kim
Maosheng Zhao
Shankar Venkataraman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Applied Materials Inc
Original Assignee
Applied Materials Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Applied Materials Inc filed Critical Applied Materials Inc
Priority to US10/346,836 priority Critical patent/US6923189B2/en
Assigned to APPLIED MATERIALS, INC. reassignment APPLIED MATERIALS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LEE, JU-HYUNG, KIM, TROY, VENKATARAMAN, SHANKAR, LAKSHMANAN, ANNAMALAI, ZHAO, MAOSHENG
Priority to PCT/US2004/000628 priority patent/WO2004066365A2/en
Priority to CN 200480000613 priority patent/CN1697892A/en
Publication of US20040139983A1 publication Critical patent/US20040139983A1/en
Application granted granted Critical
Publication of US6923189B2 publication Critical patent/US6923189B2/en
Adjusted expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J37/00Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
    • H01J37/32Gas-filled discharge tubes
    • H01J37/32431Constructional details of the reactor
    • H01J37/32798Further details of plasma apparatus not provided for in groups H01J37/3244 - H01J37/32788; special provisions for cleaning or maintenance of the apparatus
    • H01J37/32853Hygiene
    • H01J37/32862In situ cleaning of vessels and/or internal parts
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B08CLEANING
    • B08BCLEANING IN GENERAL; PREVENTION OF FOULING IN GENERAL
    • B08B7/00Cleaning by methods not provided for in a single other subclass or a single group in this subclass
    • B08B7/0035Cleaning by methods not provided for in a single other subclass or a single group in this subclass by radiant energy, e.g. UV, laser, light beam or the like
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/4401Means for minimising impurities, e.g. dust, moisture or residual gas, in the reaction chamber
    • C23C16/4405Cleaning of reactor or parts inside the reactor by using reactive gases
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S134/00Cleaning and liquid contact with solids
    • Y10S134/902Semiconductor wafer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S438/00Semiconductor device manufacturing: process
    • Y10S438/905Cleaning of reaction chamber

Definitions

  • Embodiments of the present invention generally relate to a method of cleaning a processing chamber using a remote plasma source and in situ radio frequency (RF) power.
  • RF radio frequency
  • materials such as oxides are typically deposited on a substrate in a processing chamber, such as a deposition chamber, e.g., a chemical vapor deposition (CVD) chamber.
  • a deposition chamber e.g., a chemical vapor deposition (CVD) chamber.
  • the deposition processes typically result in deposition of some of the material on the walls and components of the deposition chamber.
  • the material deposited on the chamber walls and components can affect the deposition rate from substrate to substrate and the uniformity of the deposition on the substrate.
  • etching chamber when materials such as oxides are etched from a substrate in a processing chamber, such as an etching chamber, some of the materials that are removed from the substrate typically are deposited on the walls and components of the etching chamber.
  • the material deposited on the chamber walls and components can affect the uniformity and consistency of etching processes performed in the chamber.
  • a remote plasma source can be used to provide a source of reactive species, such as fluorine radicals, that react with deposited material in a processing chamber, forming volatile compounds that can be removed from the processing chamber.
  • reactive species such as fluorine radicals
  • cleaning a processing chamber using known remote plasma sources is a time consuming process.
  • Remote plasma sources typically provide reactive species, such as free radicals, at a flow rate and an intensity that do not result in a level of free radical or ion bombardment that can damage the deposition chamber.
  • more time is required to clean a chamber when a low intensity cleaning process such as a remote plasma clean process is used.
  • a lengthy chamber cleaning period decreases the number of substrates that can be processed in a given time, since the chamber typically cannot be used for processing during the cleaning period.
  • Providing in situ radio frequency (RF) power in a processing chamber to generate a plasma of cleaning gases is another method that can be used to clean a processing chamber.
  • Reactive species generated in the plasma bombard and react with deposited material in the processing chamber, forming volatile compounds that can be removed from the deposition chamber.
  • the reactive species can also bombard the chamber and remove deposited material from the chamber surfaces.
  • the reactive species often damage the chamber due to the energy imparted to the species in the chamber.
  • the reactive species can react with the material forming the chamber lining and create undesirable contaminants that may land on and harm a substrate undergoing processing in the chamber. For example, if NF 3 is introduced into a chamber, the fluorine ions generated in the plasma can combine with aluminum used as a lining material in the deposition chamber and form particles of aluminum fluoride.
  • the removal of contaminating particles from a processing chamber is becoming increasingly important because the device sizes are becoming smaller and aspect ratios are becoming more aggressive. With smaller feature sizes and more aggressive aspect ratios, the size and number of contaminating particles must be minimized in order to maintain the performance of the device.
  • Embodiments of the present invention generally relate to methods of cleaning processing chambers, such as deposition chambers and etching chambers.
  • a method of cleaning a process chamber includes generating reactive species from a carbon and fluorine-containing gas and an oxygen source in a remote plasma source connected to the processing chamber. The reactive species are introduced into the processing chamber, and RF power is applied in the processing chamber.
  • the carbon and fluorine-containing gas is CF 4
  • the oxygen source is oxygen.
  • substantially all of the carbon and fluorine-containing gas is dissociated by the remote plasma source, and any of the carbon and fluorine-containing gas not dissociated by the remote plasma source is dissociated by the RF power applied in the processing chamber.
  • FIG. 1 is a cross sectional view of one embodiment of a deposition chamber.
  • FIG. 2 illustrates a processing sequence according to various embodiments of the invention.
  • the present invention generally provides a method for cleaning processing chambers, such as deposition chambers and etching chambers used in the fabrication of integrated circuits and semiconductor devices.
  • the deposition chambers that may be cleaned using the methods described herein include chambers that may be used to deposit oxides, such as carbon-doped silicon oxides, and other dielectric materials.
  • An example of a chamber that may be cleaned using the methods described herein is the PRODUCER® chemical vapor deposition (CVD) reactor, available from Applied Materials, Inc. of Santa Clara, Calif.
  • the PRODUCER® chemical vapor deposition reactor has two isolated processing regions that may be used to deposit carbon-doped silicon oxides and other materials.
  • a chamber having two isolated processing regions is described in U.S. Pat. No. 5,855,681, which is incorporated by reference herein.
  • the PRODUCER® chemical vapor deposition reactor has a port to which remote plasma sources may be attached.
  • a PRODUCER® chemical vapor deposition reactor with an ASTRON®ex remote plasma source available from MKS Instruments may be used in embodiments of the methods described herein.
  • one remote plasma source may be attached to a CVD reactor having two isolated processing regions such that the remote plasma source is connected to both isolated processing regions.
  • the processes described below may also be performed by using two remote plasma sources connected, such as via a tee line, to each processing region, and adjusting the flow rates accordingly.
  • the gas flow rates described below refer to flow rates experienced by the CVD reactor as a whole, i.e., both of the isolated processing regions. Thus, the gas flow rates experienced by each of the processing regions of the CVD reactor are approximately half the gas flow rates experienced by the CVD reactor as a whole. While some examples of embodiments are described with respect to cleaning a processing region of a CVD reactor that has two processing regions, the methods described herein may be used to clean a processing region of a chamber that has one or more than two processing regions.
  • FIG. 1 An example of a chamber that has two processing regions and two remote plasma sources is shown in FIG. 1 .
  • the chamber 100 has processing regions 618 and 620 .
  • One remote plasma source 800 is connected to processing region 618
  • the other remote plasma source 800 is connected to processing region 620 .
  • a heater pedestal 628 is movably disposed in each processing region 618 , 620 by a stem 626 which extends through the bottom of the chamber body 612 where it is connected to a drive system 603 .
  • Each of the processing regions 618 , 620 also preferably includes a gas distribution assembly 608 disposed through the chamber lid 604 to deliver gases into the processing regions 618 , 620 .
  • the gas distribution assembly 608 of each processing region also includes a gas inlet passage 640 which delivers gas into a shower head assembly 642 .
  • Reactive species are generated from a carbon and fluorine-containing gas and an oxygen source in a remote plasma source connected to the processing chamber, as shown in step 200 .
  • the carbon and fluorine-containing gas may be a fluorocarbon, such as CF 4 , C 2 F 4 or C 2 F 6 .
  • the ratio of the carbon and fluorine-containing gas to the oxygen source is about 2:1 to about 1:4.
  • the carbon and fluorine-containing gas may include oxygen and have the general formula C x F y O z , wherein x is an integer from 1 to 6, y is an integer from 1 to 14, and z is an integer from 1 to 4.
  • the oxygen source may be an oxidizing gas such as oxygen, ozone, or nitrous oxide.
  • the oxygen source is oxygen and the carbon and fluorine-containing gas is CF 4 .
  • the reactive species may be generated by introducing an inert gas, such as argon, into the remote plasma source and striking a plasma. After the plasma is struck, a carbon and fluorine-containing gas and an oxygen source are introduced into the remote plasma source, and reactive species from the carbon and fluorine-containing gas and an oxygen source are generated.
  • generating the reactive species includes dissociating substantially all of the carbon and fluorine-containing gas and substantially all of the oxygen source.
  • a high level of dissociation of the carbon and fluorine-containing gas and the oxygen source is achieved by applying a high power level, such as about 13 kilowatts or greater, to generate the reactive species in the remote plasma source.
  • a high power remote plasma source such as the ASTRON®ex remote plasma source can provide a power of at least about 13 kilowatts.
  • the reactive species are then introduced into the processing chamber from the remote plasma source, as shown in step 210 .
  • a carrier gas is introduced from a separate gas source into the processing chamber with the reactive species.
  • the carrier gas is an inert gas, such as helium.
  • the carrier gas is introduced into the processing chamber at a flow rate of about 100 sccm to about 1000 sccm.
  • the reactive species from the carbon and fluorine-containing gas are introduced into the processing chamber at a flow rate of about 400 sccm to about 1400 sccm.
  • the reactive species from the oxygen source are introduced into the processing chamber at a flow rate of about 400 sccm to about 1400 sccm.
  • RF power is applied in the processing chamber, as shown in step 220 .
  • the RF power is delivered to the processing region of the chamber by energizing an RF source connected between two electrodes in the processing region.
  • the two electrodes typically comprise the substrate support member or susceptor of the chamber, and the faceplate or “showerhead” through which processing gases are distributed into the processing region and which is directly connected to the RF power source.
  • the RF power is preferably provided at about 100 watts to about 900 watts at a frequency of about 13.56 MHz.
  • the RF power is preferably provided at a level such that about 95% or greater of the carbon and fluorine-containing gas is dissociated.
  • the recombination of the reactive species may occur during the transfer of the reactive species to the processing chamber or after the reactive species are introduced into the processing chamber.
  • the application of RF power in the processing chamber can regenerate reactive species after they have recombined or generate reactive species from any of the carbon and fluorine-containing gas or oxygen source that was not activated in the remote plasma source.
  • the RF power is applied for a period of time sufficient to remove material deposited on an interior surface of the chamber, such as material deposited during a previous deposition or etching process in the chamber.
  • the chamber may be cleaned by applying the RF power for about 50 seconds to about 300 seconds.
  • the reactive species react with material deposited on one or more interior surfaces of the chamber and form volatile components that can be removed from the chamber.
  • the temperature of the chamber during the cleaning may be about 100° C. to about 500° C.
  • the pressure may be about 1 torr to about 10 torr, and the spacing between the faceplate and the substrate support may be about 200 mils to about 1000 mils.
  • the cleaning process described herein is performed after the processing of each substrate in a processing region of a chamber.
  • the cleaning process may be performed after a deposition process is performed on a substrate in the chamber.
  • the cleaning process described herein may also be performed on an etching chamber, such as an eMAXTM chamber, an IPSTM chamber, a DPSTM chamber, and an ASP chamber, all of which are available from Applied Materials, Inc., of Santa Clara, Calif.
  • an etching chamber such as an eMAXTM chamber, an IPSTM chamber, a DPSTM chamber, and an ASP chamber, all of which are available from Applied Materials, Inc., of Santa Clara, Calif.
  • the chamber cleaning process described herein provides a good, efficient chamber cleaning method.
  • the remote plasma source provides a large number of reactive species, which accelerates the chamber cleaning process.
  • the in situ RF power in the chamber further accelerates the chamber cleaning process by regenerating reactive species from recombined species and/or by generating new reactive species.
  • the high power level of the remote plasma source described herein enables the use of CF 4 as a chamber cleaning gas.
  • Low power remote plasma sources typically cannot provide enough power to sufficiently dissociate CF 4 for an efficient chamber cleaning process.
  • Complete or nearly complete dissociation of fluorocarbons is also desirable because fluorocarbons are believed to have potentially negative effects on the environment.
  • Embodiments of the cleaning method described herein also provide an alternative to NF 3 -based chamber cleaning methods. While NF 3 can be used to effectively clean processing chambers, NF 3 is very expensive. Furthermore, when NF 3 was used in the place of the carbon and fluorine-containing gas and oxygen source in a cleaning method as described herein, the cleaning method was about 30 seconds longer than the method with the carbon and fluorine-containing gas and oxygen source, while the NF 3 method and the method described herein produced similar cleaning results. Thus, the method described herein enhances the throughput of the chamber, as a shorter chamber cleaning time is required.
  • a plasma was struck in an ASTRON®ex remote plasma source containing helium and connected to a PRODUCER® CVD reactor.
  • CF 4 and oxygen were then introduced into the remote plasma source and reactive species were generated.
  • the activated CF 4 was introduced into the PRODUCER® CVD reactor at a flow rate of about 1000 sccm and the activated oxygen was introduced into the reactor at a flow rate of about 1000 sccm.
  • Helium was introduced into the reactor from a separate gas source at a flow rate of about 500 sccm.
  • the temperature of the chamber was about 350° C. and the pressure in the chamber was about 1.6 torr.
  • the spacing between the faceplate and the substrate support was about 450 mils.
  • An in situ radio frequency power of about 350 watts was delivered to the processing region at a frequency of 13.56 MHz.
  • the chamber was cleaned for about 270 seconds.
  • About 1 ⁇ m of previously deposited material was removed from a dummy wafer on the substrate support during the cleaning process.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Plasma & Fusion (AREA)
  • Health & Medical Sciences (AREA)
  • Optics & Photonics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Vapour Deposition (AREA)
  • Drying Of Semiconductors (AREA)

Abstract

A method and apparatus for cleaning a processing chamber are provided. The cleaning method includes the use of a remote plasma source to generate reactive species and an in situ RF power to generate or regenerate reactive species. The reactive species are generated from a carbon and fluorine-containing gas and an oxygen source.

Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
Embodiments of the present invention generally relate to a method of cleaning a processing chamber using a remote plasma source and in situ radio frequency (RF) power.
2. Description of the Related Art
In the fabrication of integrated circuits and semiconductor devices, materials such as oxides are typically deposited on a substrate in a processing chamber, such as a deposition chamber, e.g., a chemical vapor deposition (CVD) chamber. The deposition processes typically result in deposition of some of the material on the walls and components of the deposition chamber. The material deposited on the chamber walls and components can affect the deposition rate from substrate to substrate and the uniformity of the deposition on the substrate.
Similarly, when materials such as oxides are etched from a substrate in a processing chamber, such as an etching chamber, some of the materials that are removed from the substrate typically are deposited on the walls and components of the etching chamber. The material deposited on the chamber walls and components can affect the uniformity and consistency of etching processes performed in the chamber.
Several methods of cleaning processing chambers have been developed. For example, a remote plasma source can be used to provide a source of reactive species, such as fluorine radicals, that react with deposited material in a processing chamber, forming volatile compounds that can be removed from the processing chamber. However, cleaning a processing chamber using known remote plasma sources is a time consuming process. Remote plasma sources typically provide reactive species, such as free radicals, at a flow rate and an intensity that do not result in a level of free radical or ion bombardment that can damage the deposition chamber. However, more time is required to clean a chamber when a low intensity cleaning process such as a remote plasma clean process is used. A lengthy chamber cleaning period decreases the number of substrates that can be processed in a given time, since the chamber typically cannot be used for processing during the cleaning period.
Providing in situ radio frequency (RF) power in a processing chamber to generate a plasma of cleaning gases is another method that can be used to clean a processing chamber. Reactive species generated in the plasma bombard and react with deposited material in the processing chamber, forming volatile compounds that can be removed from the deposition chamber. The reactive species can also bombard the chamber and remove deposited material from the chamber surfaces. However, the reactive species often damage the chamber due to the energy imparted to the species in the chamber. Furthermore, the reactive species can react with the material forming the chamber lining and create undesirable contaminants that may land on and harm a substrate undergoing processing in the chamber. For example, if NF3 is introduced into a chamber, the fluorine ions generated in the plasma can combine with aluminum used as a lining material in the deposition chamber and form particles of aluminum fluoride.
The removal of contaminating particles from a processing chamber is becoming increasingly important because the device sizes are becoming smaller and aspect ratios are becoming more aggressive. With smaller feature sizes and more aggressive aspect ratios, the size and number of contaminating particles must be minimized in order to maintain the performance of the device.
Therefore, there remains a need for a method of cleaning processing chambers efficiently, while minimizing contaminant generation.
SUMMARY OF THE INVENTION
Embodiments of the present invention generally relate to methods of cleaning processing chambers, such as deposition chambers and etching chambers. In one embodiment, a method of cleaning a process chamber includes generating reactive species from a carbon and fluorine-containing gas and an oxygen source in a remote plasma source connected to the processing chamber. The reactive species are introduced into the processing chamber, and RF power is applied in the processing chamber. In one embodiment, the carbon and fluorine-containing gas is CF4, and the oxygen source is oxygen. Preferably, substantially all of the carbon and fluorine-containing gas is dissociated by the remote plasma source, and any of the carbon and fluorine-containing gas not dissociated by the remote plasma source is dissociated by the RF power applied in the processing chamber.
BRIEF DESCRIPTION OF THE DRAWINGS
So that the manner in which the above recited features of the present invention can be understood in detail, a more particular description of the invention, briefly summarized above, may be had by reference to embodiments, some of which are illustrated in the appended drawings. It is to be noted, however, that the appended drawings illustrate only typical embodiments of this invention and are therefore not to be considered limiting of its scope, for the invention may admit to other equally effective embodiments.
FIG. 1 is a cross sectional view of one embodiment of a deposition chamber.
FIG. 2 illustrates a processing sequence according to various embodiments of the invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
The present invention generally provides a method for cleaning processing chambers, such as deposition chambers and etching chambers used in the fabrication of integrated circuits and semiconductor devices. The deposition chambers that may be cleaned using the methods described herein include chambers that may be used to deposit oxides, such as carbon-doped silicon oxides, and other dielectric materials.
An example of a chamber that may be cleaned using the methods described herein is the PRODUCER® chemical vapor deposition (CVD) reactor, available from Applied Materials, Inc. of Santa Clara, Calif. The PRODUCER® chemical vapor deposition reactor has two isolated processing regions that may be used to deposit carbon-doped silicon oxides and other materials. A chamber having two isolated processing regions is described in U.S. Pat. No. 5,855,681, which is incorporated by reference herein.
The PRODUCER® chemical vapor deposition reactor has a port to which remote plasma sources may be attached. A PRODUCER® chemical vapor deposition reactor with an ASTRON®ex remote plasma source available from MKS Instruments may be used in embodiments of the methods described herein.
In the embodiments described herein, one remote plasma source may be attached to a CVD reactor having two isolated processing regions such that the remote plasma source is connected to both isolated processing regions. However, the processes described below may also be performed by using two remote plasma sources connected, such as via a tee line, to each processing region, and adjusting the flow rates accordingly.
The gas flow rates described below refer to flow rates experienced by the CVD reactor as a whole, i.e., both of the isolated processing regions. Thus, the gas flow rates experienced by each of the processing regions of the CVD reactor are approximately half the gas flow rates experienced by the CVD reactor as a whole. While some examples of embodiments are described with respect to cleaning a processing region of a CVD reactor that has two processing regions, the methods described herein may be used to clean a processing region of a chamber that has one or more than two processing regions.
An example of a chamber that has two processing regions and two remote plasma sources is shown in FIG. 1. The chamber 100 has processing regions 618 and 620. One remote plasma source 800 is connected to processing region 618, and the other remote plasma source 800 is connected to processing region 620. A heater pedestal 628 is movably disposed in each processing region 618, 620 by a stem 626 which extends through the bottom of the chamber body 612 where it is connected to a drive system 603. Each of the processing regions 618, 620 also preferably includes a gas distribution assembly 608 disposed through the chamber lid 604 to deliver gases into the processing regions 618, 620. The gas distribution assembly 608 of each processing region also includes a gas inlet passage 640 which delivers gas into a shower head assembly 642.
One embodiment of a chamber cleaning method described herein is summarized in FIG. 2. Reactive species are generated from a carbon and fluorine-containing gas and an oxygen source in a remote plasma source connected to the processing chamber, as shown in step 200. The carbon and fluorine-containing gas may be a fluorocarbon, such as CF4, C2F4 or C2F6. Preferably, the ratio of the carbon and fluorine-containing gas to the oxygen source is about 2:1 to about 1:4. Alternatively, the carbon and fluorine-containing gas may include oxygen and have the general formula CxFyOz, wherein x is an integer from 1 to 6, y is an integer from 1 to 14, and z is an integer from 1 to 4. The oxygen source may be an oxidizing gas such as oxygen, ozone, or nitrous oxide. Preferably, the oxygen source is oxygen and the carbon and fluorine-containing gas is CF4.
The reactive species may be generated by introducing an inert gas, such as argon, into the remote plasma source and striking a plasma. After the plasma is struck, a carbon and fluorine-containing gas and an oxygen source are introduced into the remote plasma source, and reactive species from the carbon and fluorine-containing gas and an oxygen source are generated. Preferably, generating the reactive species includes dissociating substantially all of the carbon and fluorine-containing gas and substantially all of the oxygen source. A high level of dissociation of the carbon and fluorine-containing gas and the oxygen source is achieved by applying a high power level, such as about 13 kilowatts or greater, to generate the reactive species in the remote plasma source. A high power remote plasma source, such as the ASTRON®ex remote plasma source can provide a power of at least about 13 kilowatts.
The reactive species are then introduced into the processing chamber from the remote plasma source, as shown in step 210. Typically, a carrier gas is introduced from a separate gas source into the processing chamber with the reactive species. Preferably, the carrier gas is an inert gas, such as helium. In one embodiment, the carrier gas is introduced into the processing chamber at a flow rate of about 100 sccm to about 1000 sccm. The reactive species from the carbon and fluorine-containing gas are introduced into the processing chamber at a flow rate of about 400 sccm to about 1400 sccm. The reactive species from the oxygen source are introduced into the processing chamber at a flow rate of about 400 sccm to about 1400 sccm.
After the reactive species are introduced into the processing chamber, RF power is applied in the processing chamber, as shown in step 220. The RF power is delivered to the processing region of the chamber by energizing an RF source connected between two electrodes in the processing region. The two electrodes typically comprise the substrate support member or susceptor of the chamber, and the faceplate or “showerhead” through which processing gases are distributed into the processing region and which is directly connected to the RF power source. The RF power is preferably provided at about 100 watts to about 900 watts at a frequency of about 13.56 MHz. The RF power is preferably provided at a level such that about 95% or greater of the carbon and fluorine-containing gas is dissociated. While up to 100% of the carbon and fluorine-containing gas may be dissociated in the remote plasma source, a small amount of the reactive species may recombine to reform the carbon and fluorine-containing gas or other products that are less effective than the reactive species for cleaning the chamber. The recombination of the reactive species may occur during the transfer of the reactive species to the processing chamber or after the reactive species are introduced into the processing chamber. The application of RF power in the processing chamber can regenerate reactive species after they have recombined or generate reactive species from any of the carbon and fluorine-containing gas or oxygen source that was not activated in the remote plasma source. Typically, the RF power is applied for a period of time sufficient to remove material deposited on an interior surface of the chamber, such as material deposited during a previous deposition or etching process in the chamber. For example, the chamber may be cleaned by applying the RF power for about 50 seconds to about 300 seconds. Generally, the reactive species react with material deposited on one or more interior surfaces of the chamber and form volatile components that can be removed from the chamber.
The temperature of the chamber during the cleaning may be about 100° C. to about 500° C. The pressure may be about 1 torr to about 10 torr, and the spacing between the faceplate and the substrate support may be about 200 mils to about 1000 mils.
Preferably, the cleaning process described herein is performed after the processing of each substrate in a processing region of a chamber. For example, the cleaning process may be performed after a deposition process is performed on a substrate in the chamber.
While an embodiment of the cleaning process has been shown and described with respect to a deposition chamber, the cleaning process described herein may also be performed on an etching chamber, such as an eMAX™ chamber, an IPS™ chamber, a DPS™ chamber, and an ASP chamber, all of which are available from Applied Materials, Inc., of Santa Clara, Calif.
It is believed that the chamber cleaning process described herein provides a good, efficient chamber cleaning method. The remote plasma source provides a large number of reactive species, which accelerates the chamber cleaning process. The in situ RF power in the chamber further accelerates the chamber cleaning process by regenerating reactive species from recombined species and/or by generating new reactive species.
The high power level of the remote plasma source described herein enables the use of CF4 as a chamber cleaning gas. Low power remote plasma sources typically cannot provide enough power to sufficiently dissociate CF4 for an efficient chamber cleaning process. Complete or nearly complete dissociation of fluorocarbons is also desirable because fluorocarbons are believed to have potentially negative effects on the environment.
Embodiments of the cleaning method described herein also provide an alternative to NF3-based chamber cleaning methods. While NF3 can be used to effectively clean processing chambers, NF3 is very expensive. Furthermore, when NF3 was used in the place of the carbon and fluorine-containing gas and oxygen source in a cleaning method as described herein, the cleaning method was about 30 seconds longer than the method with the carbon and fluorine-containing gas and oxygen source, while the NF3 method and the method described herein produced similar cleaning results. Thus, the method described herein enhances the throughput of the chamber, as a shorter chamber cleaning time is required.
An example of a preferred embodiment will now be described.
EXAMPLE 1
A plasma was struck in an ASTRON®ex remote plasma source containing helium and connected to a PRODUCER® CVD reactor. CF4 and oxygen were then introduced into the remote plasma source and reactive species were generated. The activated CF4 was introduced into the PRODUCER® CVD reactor at a flow rate of about 1000 sccm and the activated oxygen was introduced into the reactor at a flow rate of about 1000 sccm. Helium was introduced into the reactor from a separate gas source at a flow rate of about 500 sccm. The temperature of the chamber was about 350° C. and the pressure in the chamber was about 1.6 torr. The spacing between the faceplate and the substrate support was about 450 mils. An in situ radio frequency power of about 350 watts was delivered to the processing region at a frequency of 13.56 MHz. The chamber was cleaned for about 270 seconds. About 1 μm of previously deposited material was removed from a dummy wafer on the substrate support during the cleaning process.
While the foregoing is directed to embodiments of the present invention, other and further embodiments of the invention may be devised without departing from the basic scope thereof, and the scope thereof is determined by the claims that follow.

Claims (13)

1. A method of cleaning a processing chamber, comprising:
generating reactive species from a carbon and fluorine-containing gas including oxygen and an oxygen source in a remote plasma source connected to the processing chamber;
introducing the reactive species into the processing chamber; and
applying radio frequency (RF) power in the processing chamber, wherein the processing chamber is used to deposit carbon-doped silicon oxides on a substrate and the generating reactive species is performed after the substrate has been treated with a deposition process in the processing chamber.
2. The method of claim 1, further comprising introducing a carrier gas into the processing chamber with the reactive species.
3. The method of claim 2, wherein the carrier gas is helium.
4. The method of claim 1, wherein the generating reactive species comprises dissociating substantially all of the carbon and fluorine-containing gas.
5. The method of claim 4, wherein the generating reactive species further comprises dissociating substantially all of the oxygen source.
6. The method of claim 1, wherein the RF power is applied such that about 95% or greater of the carbon and fluorine-containing gas is dissociated.
7. A method of cleaning a processing chamber, comprising:
generating reactive species from a carbon and fluorine-containing gas comprising oxygen and an oxygen source in a remote plasma source connected to the processing chamber;
introducing the reactive species into the processing chamber; and
applying radio frequency (RF) power in the processing chamber.
8. The method of claim 7, wherein the generating reactive species is performed after a substrate has been treated with a deposition process in the processing chamber.
9. The method of claim 8, wherein the applying RF power is performed for a period of time sufficient to remove material deposited on an interior surface of the processing chamber during the deposition process.
10. The method of claim 7, wherein the generating reactive species is performed after a substrate has been treated with an etching process in the processing chamber.
11. The method of claim 10, wherein the applying RF power is performed for a period of time sufficient to remove material deposited on an interior surface of the processing chamber during the etching process.
12. The method of claim 7, wherein the generating reactive species comprises dissociating substantially all of the carbon and fluorine-containing gas comprising oxygen.
13. The method of claim 7, wherein the RF power is applied such that about 95% or greater of the carbon and fluorine-containing gas comprising oxygen is dissociated.
US10/346,836 2003-01-16 2003-01-16 Cleaning of CVD chambers using remote source with cxfyoz based chemistry Expired - Fee Related US6923189B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US10/346,836 US6923189B2 (en) 2003-01-16 2003-01-16 Cleaning of CVD chambers using remote source with cxfyoz based chemistry
PCT/US2004/000628 WO2004066365A2 (en) 2003-01-16 2004-01-12 Cleaning of cvd chambers using remote source with cxfyoz based chemistry
CN 200480000613 CN1697892A (en) 2003-01-16 2004-01-12 Cleaning of cvd chambers using remote source with cxfyoz based chemistry

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10/346,836 US6923189B2 (en) 2003-01-16 2003-01-16 Cleaning of CVD chambers using remote source with cxfyoz based chemistry

Publications (2)

Publication Number Publication Date
US20040139983A1 US20040139983A1 (en) 2004-07-22
US6923189B2 true US6923189B2 (en) 2005-08-02

Family

ID=32712249

Family Applications (1)

Application Number Title Priority Date Filing Date
US10/346,836 Expired - Fee Related US6923189B2 (en) 2003-01-16 2003-01-16 Cleaning of CVD chambers using remote source with cxfyoz based chemistry

Country Status (3)

Country Link
US (1) US6923189B2 (en)
CN (1) CN1697892A (en)
WO (1) WO2004066365A2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070267143A1 (en) * 2006-05-16 2007-11-22 Applied Materials, Inc. In situ cleaning of CVD system exhaust
US20080065039A1 (en) * 2006-09-08 2008-03-13 Jennifer Lynn Labit Reusable diapers
US20090035945A1 (en) * 2007-07-31 2009-02-05 Renesas Technology Corp. Manufacturing method of semiconductor integrated circuit device
US11835465B2 (en) 2019-02-15 2023-12-05 Hitachi High-Tech Corporation Detecting method and detecting device of gas components and processing apparatus using detecting device of gas components

Families Citing this family (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100997964B1 (en) * 2003-06-16 2010-12-02 삼성전자주식회사 Manufacturing method of thin film transistor array panel
US20050258137A1 (en) * 2004-03-24 2005-11-24 Sawin Herbert H Remote chamber methods for removing surface deposits
US20060144820A1 (en) * 2004-12-30 2006-07-06 Sawin Herbert H Remote chamber methods for removing surface deposits
US20060144819A1 (en) * 2004-12-30 2006-07-06 Sawin Herbert H Remote chamber methods for removing surface deposits
US20070207275A1 (en) * 2006-02-21 2007-09-06 Applied Materials, Inc. Enhancement of remote plasma source clean for dielectric films
US7825038B2 (en) * 2006-05-30 2010-11-02 Applied Materials, Inc. Chemical vapor deposition of high quality flow-like silicon dioxide using a silicon containing precursor and atomic oxygen
US8232176B2 (en) 2006-06-22 2012-07-31 Applied Materials, Inc. Dielectric deposition and etch back processes for bottom up gapfill
KR100806041B1 (en) * 2006-08-29 2008-02-26 동부일렉트로닉스 주식회사 An apparatus for fabricating semiconductor device and a method of fabricating semiconductor device using the same
US7867923B2 (en) * 2007-10-22 2011-01-11 Applied Materials, Inc. High quality silicon oxide films by remote plasma CVD from disilane precursors
US8357435B2 (en) 2008-05-09 2013-01-22 Applied Materials, Inc. Flowable dielectric equipment and processes
US8980382B2 (en) 2009-12-02 2015-03-17 Applied Materials, Inc. Oxygen-doping for non-carbon radical-component CVD films
US8741788B2 (en) 2009-08-06 2014-06-03 Applied Materials, Inc. Formation of silicon oxide using non-carbon flowable CVD processes
US8449942B2 (en) 2009-11-12 2013-05-28 Applied Materials, Inc. Methods of curing non-carbon flowable CVD films
SG181670A1 (en) * 2009-12-30 2012-07-30 Applied Materials Inc Dielectric film growth with radicals produced using flexible nitrogen/hydrogen ratio
US8329262B2 (en) 2010-01-05 2012-12-11 Applied Materials, Inc. Dielectric film formation using inert gas excitation
US8647992B2 (en) 2010-01-06 2014-02-11 Applied Materials, Inc. Flowable dielectric using oxide liner
JP2013516788A (en) 2010-01-07 2013-05-13 アプライド マテリアルズ インコーポレイテッド In situ ozone curing for radical component CVD
JP2013521650A (en) 2010-03-05 2013-06-10 アプライド マテリアルズ インコーポレイテッド Conformal layer by radical component CVD
US9285168B2 (en) 2010-10-05 2016-03-15 Applied Materials, Inc. Module for ozone cure and post-cure moisture treatment
US8664127B2 (en) 2010-10-15 2014-03-04 Applied Materials, Inc. Two silicon-containing precursors for gapfill enhancing dielectric liner
US10283321B2 (en) 2011-01-18 2019-05-07 Applied Materials, Inc. Semiconductor processing system and methods using capacitively coupled plasma
US8450191B2 (en) 2011-01-24 2013-05-28 Applied Materials, Inc. Polysilicon films by HDP-CVD
US8716154B2 (en) 2011-03-04 2014-05-06 Applied Materials, Inc. Reduced pattern loading using silicon oxide multi-layers
US8445078B2 (en) 2011-04-20 2013-05-21 Applied Materials, Inc. Low temperature silicon oxide conversion
US8466073B2 (en) 2011-06-03 2013-06-18 Applied Materials, Inc. Capping layer for reduced outgassing
US9404178B2 (en) 2011-07-15 2016-08-02 Applied Materials, Inc. Surface treatment and deposition for reduced outgassing
US8617989B2 (en) 2011-09-26 2013-12-31 Applied Materials, Inc. Liner property improvement
US8551891B2 (en) 2011-10-04 2013-10-08 Applied Materials, Inc. Remote plasma burn-in
US8889566B2 (en) 2012-09-11 2014-11-18 Applied Materials, Inc. Low cost flowable dielectric films
US9018108B2 (en) 2013-01-25 2015-04-28 Applied Materials, Inc. Low shrinkage dielectric films
US20150361547A1 (en) * 2014-06-13 2015-12-17 Taiwan Semiconductor Manufacturing Co., Ltd Method and apparatus for cleaning chemical vapor deposition chamber
US9412581B2 (en) 2014-07-16 2016-08-09 Applied Materials, Inc. Low-K dielectric gapfill by flowable deposition
US20160225652A1 (en) 2015-02-03 2016-08-04 Applied Materials, Inc. Low temperature chuck for plasma processing systems
KR20210116679A (en) * 2019-02-11 2021-09-27 어플라이드 머티어리얼스, 인코포레이티드 Method for cleaning the process chamber
CN110571121B (en) * 2019-09-17 2022-08-26 江苏鲁汶仪器有限公司 Ion beam etching device and method for self-cleaning by adopting remote plasma

Citations (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4820377A (en) 1987-07-16 1989-04-11 Texas Instruments Incorporated Method for cleanup processing chamber and vacuum process module
US5158644A (en) 1986-12-19 1992-10-27 Applied Materials, Inc. Reactor chamber self-cleaning process
EP0555546A1 (en) 1992-01-15 1993-08-18 International Business Machines Corporation Plasma CVD apparatus and processes
US5454903A (en) * 1993-10-29 1995-10-03 Applied Materials, Inc. Plasma cleaning of a CVD or etch reactor using helium for plasma stabilization
EP0697467A1 (en) 1994-07-21 1996-02-21 Applied Materials, Inc. Method and apparatus for cleaning a deposition chamber
US5788778A (en) 1996-09-16 1998-08-04 Applied Komatsu Technology, Inc. Deposition chamber cleaning technique using a high power remote excitation source
US5886473A (en) 1996-09-02 1999-03-23 Hitachi, Ltd. Surface wave plasma processing apparatus
US6107192A (en) 1997-12-30 2000-08-22 Applied Materials, Inc. Reactive preclean prior to metallization for sub-quarter micron application
US6164295A (en) 1996-05-01 2000-12-26 Kabushiki Kaisha Toshiba CVD apparatus with high throughput and cleaning method therefor
JP2001118692A (en) * 1999-10-15 2001-04-27 Matsushita Electric Works Ltd Lighting apparatus of discharge lamp
US6271148B1 (en) 1997-04-23 2001-08-07 Applied Materials, Inc. Method for improved remote microwave plasma source for use with substrate processing system
US6274058B1 (en) 1997-07-11 2001-08-14 Applied Materials, Inc. Remote plasma cleaning method for processing chambers
US20010025645A1 (en) * 2000-03-02 2001-10-04 Jusung Engineering Co., Ltd. Apparatus for fabricating semiconductor device and method of cleaning the same
WO2002012587A2 (en) 2000-08-08 2002-02-14 Tokyo Electron Limited Processing apparatus and cleaning method
US6379575B1 (en) 1997-10-21 2002-04-30 Applied Materials, Inc. Treatment of etching chambers using activated cleaning gas
US20020052114A1 (en) 2000-03-30 2002-05-02 Lam Research Corporation Enhanced resist strip in a dielectric etcher using downstream plasma
US20020104467A1 (en) 1999-02-04 2002-08-08 Applied Materials, Inc. Accelerated plasma clean
US6432255B1 (en) * 2000-01-31 2002-08-13 Applied Materials, Inc. Method and apparatus for enhancing chamber cleaning
US6437512B1 (en) 2000-05-31 2002-08-20 Nanya Technology Corporation Plasma generator
US20020117473A1 (en) 1999-08-31 2002-08-29 Toshihiro Yanase Method and apparatus for plasma processing
WO2002078073A1 (en) 2001-03-22 2002-10-03 Research Institute Of Innovative Technology For The Earth Method of cleaning cvd device and cleaning device therefor
US6461975B1 (en) 1999-10-26 2002-10-08 Samsung Electronics Co., Ltd. Method of etching insulating layer in semiconductor device
US6569257B1 (en) * 2000-11-09 2003-05-27 Applied Materials Inc. Method for cleaning a process chamber
US6736147B2 (en) 2000-01-18 2004-05-18 Asm Japan K.K. Semiconductor-processing device provided with a remote plasma source for self-cleaning

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3736147A (en) * 1971-04-05 1973-05-29 Coca Cola Co Process for preparing protein products

Patent Citations (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5158644A (en) 1986-12-19 1992-10-27 Applied Materials, Inc. Reactor chamber self-cleaning process
US4820377A (en) 1987-07-16 1989-04-11 Texas Instruments Incorporated Method for cleanup processing chamber and vacuum process module
EP0555546A1 (en) 1992-01-15 1993-08-18 International Business Machines Corporation Plasma CVD apparatus and processes
US5454903A (en) * 1993-10-29 1995-10-03 Applied Materials, Inc. Plasma cleaning of a CVD or etch reactor using helium for plasma stabilization
EP0697467A1 (en) 1994-07-21 1996-02-21 Applied Materials, Inc. Method and apparatus for cleaning a deposition chamber
US6164295A (en) 1996-05-01 2000-12-26 Kabushiki Kaisha Toshiba CVD apparatus with high throughput and cleaning method therefor
US5886473A (en) 1996-09-02 1999-03-23 Hitachi, Ltd. Surface wave plasma processing apparatus
US5788778A (en) 1996-09-16 1998-08-04 Applied Komatsu Technology, Inc. Deposition chamber cleaning technique using a high power remote excitation source
US6271148B1 (en) 1997-04-23 2001-08-07 Applied Materials, Inc. Method for improved remote microwave plasma source for use with substrate processing system
US6274058B1 (en) 1997-07-11 2001-08-14 Applied Materials, Inc. Remote plasma cleaning method for processing chambers
US6379575B1 (en) 1997-10-21 2002-04-30 Applied Materials, Inc. Treatment of etching chambers using activated cleaning gas
US6107192A (en) 1997-12-30 2000-08-22 Applied Materials, Inc. Reactive preclean prior to metallization for sub-quarter micron application
US20020104467A1 (en) 1999-02-04 2002-08-08 Applied Materials, Inc. Accelerated plasma clean
US20020117473A1 (en) 1999-08-31 2002-08-29 Toshihiro Yanase Method and apparatus for plasma processing
JP2001118692A (en) * 1999-10-15 2001-04-27 Matsushita Electric Works Ltd Lighting apparatus of discharge lamp
US6461975B1 (en) 1999-10-26 2002-10-08 Samsung Electronics Co., Ltd. Method of etching insulating layer in semiconductor device
US6736147B2 (en) 2000-01-18 2004-05-18 Asm Japan K.K. Semiconductor-processing device provided with a remote plasma source for self-cleaning
US6432255B1 (en) * 2000-01-31 2002-08-13 Applied Materials, Inc. Method and apparatus for enhancing chamber cleaning
US20010025645A1 (en) * 2000-03-02 2001-10-04 Jusung Engineering Co., Ltd. Apparatus for fabricating semiconductor device and method of cleaning the same
US6435197B2 (en) * 2000-03-02 2002-08-20 Jusung Engineering Co., Ltd. Method of cleaning a semiconductor fabricating apparatus
US20020052114A1 (en) 2000-03-30 2002-05-02 Lam Research Corporation Enhanced resist strip in a dielectric etcher using downstream plasma
US6437512B1 (en) 2000-05-31 2002-08-20 Nanya Technology Corporation Plasma generator
WO2002012587A2 (en) 2000-08-08 2002-02-14 Tokyo Electron Limited Processing apparatus and cleaning method
US6569257B1 (en) * 2000-11-09 2003-05-27 Applied Materials Inc. Method for cleaning a process chamber
WO2002078073A1 (en) 2001-03-22 2002-10-03 Research Institute Of Innovative Technology For The Earth Method of cleaning cvd device and cleaning device therefor
EP1304731A1 (en) 2001-03-22 2003-04-23 Research Institute of Innovative Technology for the Earth Method of cleaning cvd device and cleaning device therefor

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
U.S. Appl. No. 09/710,357, filed Nov. 9, 2000.

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070267143A1 (en) * 2006-05-16 2007-11-22 Applied Materials, Inc. In situ cleaning of CVD system exhaust
US20090044699A1 (en) * 2006-05-16 2009-02-19 Applied Materials, Inc. In Situ Cleaning of CVD System Exhaust
US8343317B2 (en) 2006-05-16 2013-01-01 Applied Materials, Inc. In situ cleaning of CVD System exhaust
US20080065039A1 (en) * 2006-09-08 2008-03-13 Jennifer Lynn Labit Reusable diapers
US20090035945A1 (en) * 2007-07-31 2009-02-05 Renesas Technology Corp. Manufacturing method of semiconductor integrated circuit device
US7790478B2 (en) * 2007-07-31 2010-09-07 Renesas Technology Corp. Manufacturing method of semiconductor integrated circuit device
CN101359586B (en) * 2007-07-31 2011-09-14 瑞萨电子株式会社 Manufacturing method of semiconductor integrated circuit device
US11835465B2 (en) 2019-02-15 2023-12-05 Hitachi High-Tech Corporation Detecting method and detecting device of gas components and processing apparatus using detecting device of gas components

Also Published As

Publication number Publication date
WO2004066365A3 (en) 2004-11-04
WO2004066365A2 (en) 2004-08-05
CN1697892A (en) 2005-11-16
US20040139983A1 (en) 2004-07-22

Similar Documents

Publication Publication Date Title
US6923189B2 (en) Cleaning of CVD chambers using remote source with cxfyoz based chemistry
US6902629B2 (en) Method for cleaning a process chamber
KR102158307B1 (en) Plasma treatment process to improve in-situ chamber cleaning efficiency in plasma processing chamber
US10916407B2 (en) Conditioning remote plasma source for enhanced performance having repeatable etch and deposition rates
US7465357B2 (en) Computer-readable medium that contains software for executing a method for cleaning a CVD chamber
US8591659B1 (en) Plasma clean method for deposition chamber
US5454903A (en) Plasma cleaning of a CVD or etch reactor using helium for plasma stabilization
US20060090773A1 (en) Sulfur hexafluoride remote plasma source clean
US20070207275A1 (en) Enhancement of remote plasma source clean for dielectric films
JPH0831451B2 (en) Cleaning method for plasma reactor
JP2002033289A (en) Fluorine process for cleaning semiconductor process chamber
US10892143B2 (en) Technique to prevent aluminum fluoride build up on the heater
US6360754B2 (en) Method of protecting quartz hardware from etching during plasma-enhanced cleaning of a semiconductor processing chamber
JP2009200182A (en) Attached object removing method and substrate treatment method
JP2012243958A (en) Plasma processing method
KR20210116679A (en) Method for cleaning the process chamber
US20060054183A1 (en) Method to reduce plasma damage during cleaning of semiconductor wafer processing chamber
JPH0529285A (en) Cleaning method and semiconductor manufacturing device
US20160133441A1 (en) Etch enhancement via controlled introduction of chamber contaminants
WO2003014413A1 (en) Treating device and cleaning method therefor

Legal Events

Date Code Title Description
AS Assignment

Owner name: APPLIED MATERIALS, INC., CALIFORNIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LAKSHMANAN, ANNAMALAI;LEE, JU-HYUNG;KIM, TROY;AND OTHERS;REEL/FRAME:013689/0930;SIGNING DATES FROM 20030113 TO 20030115

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees

Free format text: PATENT EXPIRED FOR FAILURE TO PAY MAINTENANCE FEES (ORIGINAL EVENT CODE: EXP.)

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362

FP Expired due to failure to pay maintenance fee

Effective date: 20170802